US4227883A - Process and composition for cleaning or de-oiling textile materials - Google Patents
Process and composition for cleaning or de-oiling textile materials Download PDFInfo
- Publication number
- US4227883A US4227883A US05/956,627 US95662778A US4227883A US 4227883 A US4227883 A US 4227883A US 95662778 A US95662778 A US 95662778A US 4227883 A US4227883 A US 4227883A
- Authority
- US
- United States
- Prior art keywords
- redeposition
- additive
- composition
- monoketone
- perchloroethylene
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 28
- 239000004753 textile Substances 0.000 title claims abstract description 27
- 238000000034 method Methods 0.000 title claims abstract description 15
- 238000004140 cleaning Methods 0.000 title claims description 10
- 239000000463 material Substances 0.000 title description 3
- CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical group ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 claims abstract description 38
- 239000000654 additive Substances 0.000 claims abstract description 21
- 230000000996 additive effect Effects 0.000 claims abstract description 21
- 238000005108 dry cleaning Methods 0.000 claims abstract description 15
- 239000000126 substance Substances 0.000 claims abstract description 11
- 238000009835 boiling Methods 0.000 claims abstract description 8
- 229920002994 synthetic fiber Polymers 0.000 claims abstract description 8
- 238000010186 staining Methods 0.000 claims abstract description 6
- XNLICIUVMPYHGG-UHFFFAOYSA-N pentan-2-one Chemical group CCCC(C)=O XNLICIUVMPYHGG-UHFFFAOYSA-N 0.000 claims description 13
- FDPIMTJIUBPUKL-UHFFFAOYSA-N pentan-3-one Chemical compound CCC(=O)CC FDPIMTJIUBPUKL-UHFFFAOYSA-N 0.000 claims description 9
- 230000000694 effects Effects 0.000 claims description 8
- -1 fluoro- Chemical class 0.000 claims description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 7
- 150000002576 ketones Chemical class 0.000 claims description 6
- 239000012744 reinforcing agent Substances 0.000 claims description 6
- PJGSXYOJTGTZAV-UHFFFAOYSA-N pinacolone Chemical group CC(=O)C(C)(C)C PJGSXYOJTGTZAV-UHFFFAOYSA-N 0.000 claims description 5
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 claims description 3
- 125000004649 C2-C8 alkynyl group Chemical group 0.000 claims description 3
- 239000002216 antistatic agent Substances 0.000 claims description 3
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 3
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 3
- 125000005119 alkyl cycloalkyl group Chemical group 0.000 claims 2
- 150000001875 compounds Chemical class 0.000 abstract description 3
- 229950011008 tetrachloroethylene Drugs 0.000 description 32
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 13
- 229920000742 Cotton Polymers 0.000 description 13
- 239000003795 chemical substances by application Substances 0.000 description 11
- 229920000728 polyester Polymers 0.000 description 11
- 150000001408 amides Chemical class 0.000 description 10
- HCFAJYNVAYBARA-UHFFFAOYSA-N 4-heptanone Chemical compound CCCC(=O)CCC HCFAJYNVAYBARA-UHFFFAOYSA-N 0.000 description 8
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 6
- HXVNBWAKAOHACI-UHFFFAOYSA-N 2,4-dimethyl-3-pentanone Chemical compound CC(C)C(=O)C(C)C HXVNBWAKAOHACI-UHFFFAOYSA-N 0.000 description 5
- 238000005303 weighing Methods 0.000 description 5
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
- 239000004952 Polyamide Substances 0.000 description 4
- 239000000835 fiber Substances 0.000 description 4
- 229920002647 polyamide Polymers 0.000 description 4
- 239000000758 substrate Substances 0.000 description 3
- OXHNLMTVIGZXSG-UHFFFAOYSA-N 1-Methylpyrrole Chemical compound CN1C=CC=C1 OXHNLMTVIGZXSG-UHFFFAOYSA-N 0.000 description 2
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 2
- QQZOPKMRPOGIEB-UHFFFAOYSA-N 2-Oxohexane Chemical compound CCCCC(C)=O QQZOPKMRPOGIEB-UHFFFAOYSA-N 0.000 description 2
- ZIXLDMFVRPABBX-UHFFFAOYSA-N 2-methylcyclopentan-1-one Chemical compound CC1CCCC1=O ZIXLDMFVRPABBX-UHFFFAOYSA-N 0.000 description 2
- SYBYTAAJFKOIEJ-UHFFFAOYSA-N 3-Methylbutan-2-one Chemical compound CC(C)C(C)=O SYBYTAAJFKOIEJ-UHFFFAOYSA-N 0.000 description 2
- FFWSICBKRCICMR-UHFFFAOYSA-N 5-methyl-2-hexanone Chemical compound CC(C)CCC(C)=O FFWSICBKRCICMR-UHFFFAOYSA-N 0.000 description 2
- QSJXEFYPDANLFS-UHFFFAOYSA-N Diacetyl Chemical compound CC(=O)C(C)=O QSJXEFYPDANLFS-UHFFFAOYSA-N 0.000 description 2
- DXVYLFHTJZWTRF-UHFFFAOYSA-N Ethyl isobutyl ketone Chemical compound CCC(=O)CC(C)C DXVYLFHTJZWTRF-UHFFFAOYSA-N 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- YRKCREAYFQTBPV-UHFFFAOYSA-N acetylacetone Chemical compound CC(=O)CC(C)=O YRKCREAYFQTBPV-UHFFFAOYSA-N 0.000 description 2
- 239000012736 aqueous medium Substances 0.000 description 2
- VQFAIAKCILWQPZ-UHFFFAOYSA-N bromoacetone Chemical compound CC(=O)CBr VQFAIAKCILWQPZ-UHFFFAOYSA-N 0.000 description 2
- BGTOWKSIORTVQH-UHFFFAOYSA-N cyclopentanone Chemical compound O=C1CCCC1 BGTOWKSIORTVQH-UHFFFAOYSA-N 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- 239000002609 medium Substances 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- XAMUDJHXFNRLCY-UHFFFAOYSA-N phenthoate Chemical compound CCOC(=O)C(SP(=S)(OC)OC)C1=CC=CC=C1 XAMUDJHXFNRLCY-UHFFFAOYSA-N 0.000 description 2
- 229920000151 polyglycol Polymers 0.000 description 2
- 239000010695 polyglycol Substances 0.000 description 2
- 239000002689 soil Substances 0.000 description 2
- 230000006641 stabilisation Effects 0.000 description 2
- 238000011105 stabilization Methods 0.000 description 2
- 239000012209 synthetic fiber Substances 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- ULPMRIXXHGUZFA-UHFFFAOYSA-N (R)-4-Methyl-3-hexanone Natural products CCC(C)C(=O)CC ULPMRIXXHGUZFA-UHFFFAOYSA-N 0.000 description 1
- CSVFWMMPUJDVKH-UHFFFAOYSA-N 1,1-dichloropropan-2-one Chemical compound CC(=O)C(Cl)Cl CSVFWMMPUJDVKH-UHFFFAOYSA-N 0.000 description 1
- CCXQVBSQUQCEEO-UHFFFAOYSA-N 1-bromobutan-2-one Chemical compound CCC(=O)CBr CCXQVBSQUQCEEO-UHFFFAOYSA-N 0.000 description 1
- LYGCEXZUGZMYCQ-UHFFFAOYSA-N 1-cyclopropylpropane-1,2-dione Chemical compound CC(=O)C(=O)C1CC1 LYGCEXZUGZMYCQ-UHFFFAOYSA-N 0.000 description 1
- FXNDIJDIPNCZQJ-UHFFFAOYSA-N 2,4,4-trimethylpent-1-ene Chemical group CC(=C)CC(C)(C)C FXNDIJDIPNCZQJ-UHFFFAOYSA-N 0.000 description 1
- AKRJXOYALOGLHQ-UHFFFAOYSA-N 2-methylheptan-4-one Chemical compound CCCC(=O)CC(C)C AKRJXOYALOGLHQ-UHFFFAOYSA-N 0.000 description 1
- ZGHFDIIVVIFNPS-UHFFFAOYSA-N 3-Methyl-3-buten-2-one Chemical compound CC(=C)C(C)=O ZGHFDIIVVIFNPS-UHFFFAOYSA-N 0.000 description 1
- PFCHFHIRKBAQGU-UHFFFAOYSA-N 3-hexanone Chemical compound CCCC(=O)CC PFCHFHIRKBAQGU-UHFFFAOYSA-N 0.000 description 1
- SHOJXDKTYKFBRD-UHFFFAOYSA-N 4-Methyl-3-penten-2-one, 9CI Chemical compound CC(C)=CC(C)=O SHOJXDKTYKFBRD-UHFFFAOYSA-N 0.000 description 1
- RNDVGJZUHCKENF-UHFFFAOYSA-N 5-hexen-2-one Chemical compound CC(=O)CCC=C RNDVGJZUHCKENF-UHFFFAOYSA-N 0.000 description 1
- DHRKMWTXCRFAIT-UHFFFAOYSA-N CC(C)C(C(C)C)=O.CC(C=CC)=O Chemical compound CC(C)C(C(C)C)=O.CC(C=CC)=O DHRKMWTXCRFAIT-UHFFFAOYSA-N 0.000 description 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
- 101100386054 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) CYS3 gene Proteins 0.000 description 1
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 238000010009 beating Methods 0.000 description 1
- TZCGKHSDBLKXIQ-UHFFFAOYSA-N bis(1-ethyl-2-methylcyclobutyl)methanone Chemical compound C1CC(C)C1(CC)C(=O)C1(CC)CCC1C TZCGKHSDBLKXIQ-UHFFFAOYSA-N 0.000 description 1
- WCAQUWHPSCDOLE-UHFFFAOYSA-N bis(1-ethyl-2-methylcyclopropyl)methanone Chemical compound C1C(C)C1(CC)C(=O)C1(CC)CC1C WCAQUWHPSCDOLE-UHFFFAOYSA-N 0.000 description 1
- 238000005282 brightening Methods 0.000 description 1
- XRGPFNGLRSIPSA-UHFFFAOYSA-N butyn-2-one Chemical compound CC(=O)C#C XRGPFNGLRSIPSA-UHFFFAOYSA-N 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- BULLHNJGPPOUOX-UHFFFAOYSA-N chloroacetone Chemical compound CC(=O)CCl BULLHNJGPPOUOX-UHFFFAOYSA-N 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- BADXJIPKFRBFOT-UHFFFAOYSA-N dimedone Chemical compound CC1(C)CC(=O)CC(=O)C1 BADXJIPKFRBFOT-UHFFFAOYSA-N 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- YRIUSKIDOIARQF-UHFFFAOYSA-N dodecyl benzenesulfonate Chemical compound CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 YRIUSKIDOIARQF-UHFFFAOYSA-N 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 238000007046 ethoxylation reaction Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- JMMWKPVZQRWMSS-UHFFFAOYSA-N isopropanol acetate Natural products CC(C)OC(C)=O JMMWKPVZQRWMSS-UHFFFAOYSA-N 0.000 description 1
- 229940011051 isopropyl acetate Drugs 0.000 description 1
- GWYFCOCPABKNJV-UHFFFAOYSA-N isovaleric acid Chemical compound CC(C)CC(O)=O GWYFCOCPABKNJV-UHFFFAOYSA-N 0.000 description 1
- 239000006233 lamp black Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 239000010705 motor oil Substances 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 150000004893 oxazines Chemical class 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 230000001172 regenerating effect Effects 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 101150035983 str1 gene Proteins 0.000 description 1
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000004078 waterproofing Methods 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06L—DRY-CLEANING, WASHING OR BLEACHING FIBRES, FILAMENTS, THREADS, YARNS, FABRICS, FEATHERS OR MADE-UP FIBROUS GOODS; BLEACHING LEATHER OR FURS
- D06L1/00—Dry-cleaning or washing fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods
- D06L1/02—Dry-cleaning or washing fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods using organic solvents
- D06L1/06—De-sizing
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06L—DRY-CLEANING, WASHING OR BLEACHING FIBRES, FILAMENTS, THREADS, YARNS, FABRICS, FEATHERS OR MADE-UP FIBROUS GOODS; BLEACHING LEATHER OR FURS
- D06L1/00—Dry-cleaning or washing fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods
- D06L1/02—Dry-cleaning or washing fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods using organic solvents
- D06L1/04—Dry-cleaning or washing fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods using organic solvents combined with specific additives
Definitions
- the present invention relates to a process for dry cleaning and de-oiling textiles, for the purpose of preventing stains from being redeposited on a textile substrate of natural, artificial or synthetic fibers or a mixture of such fibers, and thus holding the soil or staining substances of the substrate in suspension in the liquid bath in the course of the cleaning and de-oiling operation.
- the factors which may be involved in this redeposition are multiple and the complexity of the phenomenon depends mainly on the diversity of the fibers involved in the same cleaning baths, and on the hygrometry of the ambient atmosphere.
- these agents whether those used in aqueous medium or those used in an organic solvent medium have the drawback of not being distillable. Accordingly, when regenerating the spent perchloroethylene by distillation, such agents remain at the bottom of the still with the soils or stains and other heavy residual substances, and can therefore no longer be recovered. In other words, these anti-redeposition agents of the prior art must be systematically added each time that the perchloroethylene is regenerated from the soiled solvent medium.
- French Pat. No. 1.536.343 describes a dry cleaning process with comprises using perchloroethylene containing a lower alkanedione, such as 2,3-butanedione, 2,4-pentanedione, 2,5,-hexanedione or a cycloalkanedione such as 5,5-dimethyl 1,3-cyclohexanedione, in order to prevent polyvalent metal ion impurities from being deposited and which are responsible for the decrease in brightness of the materials cleaned, but have no active participation (or without taking any active part or share) in the conventional greying phenomenon.
- a lower alkanedione such as 2,3-butanedione, 2,4-pentanedione, 2,5,-hexanedione or a cycloalkanedione such as 5,5-dimethyl 1,3-cyclohexanedione
- the object of the present invention is to avoid redeposition and thus very considerably limit the "greying" phenomenon, during dry cleaning or de-oiling of textiles of synthetic artificial, natural or mixed fibers, while making it possible to recover and re-use the anti-redeposition agent of the invention, by distillation with the perchloroethylene in each bath regeneration stage.
- the invention therefore concerns a process for anti-redeposition of stains, when dry cleaning or de-oiling, by means of suitably stabilized perchloroethylene, the process being characterized in that in order to observe the desired effect of limiting the "greying" phenomenon of the textiles, a sufficient amount is added of an additive represented by at least one monoketone having a boiling point not in excess of 160° C., and preferably less than 140° C.
- ketones may be selected from those represented by the general formula: ##STR1## where R and R', which may be identical or different, represent C 1 -C 8 alkyl, C 1 -C 8 fluoro-, chloro- or bromo-alkyl, C 2 -C 8 alkenyl, C 2 -C 8 alkynyl, or a cyclopropyl group, or taken jointly R and R' represent a C 5 -C 6 cycloalkyl group, a C 5 -C 8 alkycycloalkyl or a C 5 -C 8 alkenylcycloalkyl group.
- the desired anti-redeposition effect becomes appreciable when at least 0.5 by weight of the monoketone additive is added to the stabilized perchloroethylene, and the optimum effect is generally secured for a concentration of up to 8% by weight, and preferably from 2 to 5% by weight.
- the perchloroethylene may be stablized by any suitable stabilization agent, in particular those which are compatible with the presence of the above defined ketone additive such as, inter alia, and without this list of compounds being limiting: butylene oxide, triethylamine, tertio-butanol, N-methylpyrrole, n-butanol, diisobutylene, isopropyl acetate and more particularly epichlorohydrin, taken separately or in the form of a mixture of at least two of such compounds.
- suitable stabilization agent in particular those which are compatible with the presence of the above defined ketone additive such as, inter alia, and without this list of compounds being limiting: butylene oxide, triethylamine, tertio-butanol, N-methylpyrrole, n-butanol, diisobutylene, isopropyl acetate and more particularly epichlorohydrin, taken separately or in the form of a mixture of at least two of such compounds
- the process of the invention may comprise the addition of water in proportions which may be up to about 5 to 6%, and more particulary from 2 to 3% by weight relative to the textiles to be cleaned.
- This water may originate from the moisture provided by the textiles themselves and/or by the commercial cleaning reinforcing agents which contain between 4 and 30% and usually from 8 to 14% of their weight of water.
- additional amounts of water are added (about 2 to 4% by weight relative to the textiles to be cleaned) to the cleaning bath containing the reinforcing agents in order to improve the cleaning effect relative to so-called "meager" soiling substances.
- the ketone used includes or consists essentially of 3--3 dimethyl 2-butanone.
- the textile samples were centrifuged and dried at a temperature of 60° C. in a ventilated oven.
- the starting perchlorethylene was stabilized by 0.0025% of triethylamine, 0.002% of N-methylpyrrole and 0.02% of n-butanol.
- Example 2 Using a dry-cleaning composition consisting essentially of 95% perchloroethylene stabilized as in Example 2, and 5% 2-pentanone, and employing the same procedural steps as in Example 1, the following results were obtained:
- Example 6 was repeated with 3-pentanone instead of 2-pentanone as the anti-redeposition additive.
- Table 7 illustrates the results obtained.
- Example 8 was repeated but with only 2.5% instead of 5% 4-methyl 2-pentanone, in the dry cleaning composition.
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Detergent Compositions (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
Process for anti-redeposition of staining substances on textiles of natural, synthetic or artificial fibers or mixtures thereof in the course of operations of dry cleaning or de-oiling by means of suitably stabilized perchloroethylene in which a sufficient amount of an additive represented by at least one monoketone compound having a boiling point below or equal to 160 DEG C. and, preferably lower than 140 DEG C., is added as an anti-redeposition additive.
Description
The present invention relates to a process for dry cleaning and de-oiling textiles, for the purpose of preventing stains from being redeposited on a textile substrate of natural, artificial or synthetic fibers or a mixture of such fibers, and thus holding the soil or staining substances of the substrate in suspension in the liquid bath in the course of the cleaning and de-oiling operation.
The invention also relates to a perchloroethylene-base composition for dry cleaning and de-oiling textiles and means for preventing the stains on a substrate from being redeposited thereon.
It is known that, when carrying out dry cleaning or de-oiling operations by means of perchloroethylene, on woven or knitted textiles, the stains which are removed from the textiles have a tendency to be redeposited on the textiles, particularly when the perchloroethylene is not regularly regenerated. This accentuates the phenomenon of "greying" of the textiles, which is more easily observed on white or light-colored fabrics.
The factors which may be involved in this redeposition are multiple and the complexity of the phenomenon depends mainly on the diversity of the fibers involved in the same cleaning baths, and on the hygrometry of the ambient atmosphere.
Various anti-redeposition agents have already been proposed for washing textiles in aqueous medium, in particular cellulose derivatives.
For the purpose of cleaning in organic solvent meduim, it is known from French Pat. No. 1.386.783 and its addition No. 89.341 that certain reinforcing agents have an anti-redeposition action, in particular, oxazines or substituted amides having more than 10 carbon atoms.
However, these agents whether those used in aqueous medium or those used in an organic solvent medium have the drawback of not being distillable. Accordingly, when regenerating the spent perchloroethylene by distillation, such agents remain at the bottom of the still with the soils or stains and other heavy residual substances, and can therefore no longer be recovered. In other words, these anti-redeposition agents of the prior art must be systematically added each time that the perchloroethylene is regenerated from the soiled solvent medium.
On the other hand, French Pat. No. 1.536.343 describes a dry cleaning process with comprises using perchloroethylene containing a lower alkanedione, such as 2,3-butanedione, 2,4-pentanedione, 2,5,-hexanedione or a cycloalkanedione such as 5,5-dimethyl 1,3-cyclohexanedione, in order to prevent polyvalent metal ion impurities from being deposited and which are responsible for the decrease in brightness of the materials cleaned, but have no active participation (or without taking any active part or share) in the conventional greying phenomenon.
The object of the present invention is to avoid redeposition and thus very considerably limit the "greying" phenomenon, during dry cleaning or de-oiling of textiles of synthetic artificial, natural or mixed fibers, while making it possible to recover and re-use the anti-redeposition agent of the invention, by distillation with the perchloroethylene in each bath regeneration stage.
The applicants have surprisingly found that it was possible very substantially to reduce the redeposition of staining matter, by using, in suitably stabilized perchloroethylene, at least one monoketone additive having a boiling point below or equal to 160° C. under normal pressure.
The invention therefore concerns a process for anti-redeposition of stains, when dry cleaning or de-oiling, by means of suitably stabilized perchloroethylene, the process being characterized in that in order to observe the desired effect of limiting the "greying" phenomenon of the textiles, a sufficient amount is added of an additive represented by at least one monoketone having a boiling point not in excess of 160° C., and preferably less than 140° C.
Such ketones may be selected from those represented by the general formula: ##STR1## where R and R', which may be identical or different, represent C1 -C8 alkyl, C1 -C8 fluoro-, chloro- or bromo-alkyl, C2 -C8 alkenyl, C2 -C8 alkynyl, or a cyclopropyl group, or taken jointly R and R' represent a C5 -C6 cycloalkyl group, a C5 -C8 alkycycloalkyl or a C5 -C8 alkenylcycloalkyl group.
The desired anti-redeposition effect becomes appreciable when at least 0.5 by weight of the monoketone additive is added to the stabilized perchloroethylene, and the optimum effect is generally secured for a concentration of up to 8% by weight, and preferably from 2 to 5% by weight.
The perchloroethylene may be stablized by any suitable stabilization agent, in particular those which are compatible with the presence of the above defined ketone additive such as, inter alia, and without this list of compounds being limiting: butylene oxide, triethylamine, tertio-butanol, N-methylpyrrole, n-butanol, diisobutylene, isopropyl acetate and more particularly epichlorohydrin, taken separately or in the form of a mixture of at least two of such compounds.
The anti-redeposition process according to the invention may also include the addition of auxiliary substances which are currently employed in dry cleaning, for example, cleaning reinforcing agents represented by anionic, cationic or non-ionic surface active agents, such as: alkysulphonates, alkylarylsulphonates, more particularly Ca dodecylbenzenesulphonate, products of ethoxylation of fatty alcohols and fatty acids, fatty alcohol sulphates, petroleum sulphonates, alkyl polyglycol ethers, alkylphenol polyglycol ethers, more particularly oxyethylenated nonylphenol having 12 ethylene oxide mols, color brightening agents, finishing agents, anti-static agents and water-proofing agents. Each of these auxiliary substances may be used in the usual proportions, for example from 1 to 10 g per liter of perchloroethylene-based bath, insofar as it is compatible with the presence of the monoketone additive of the invention as defined hereinabove.
In addition, the process of the invention may comprise the addition of water in proportions which may be up to about 5 to 6%, and more particulary from 2 to 3% by weight relative to the textiles to be cleaned. This water may originate from the moisture provided by the textiles themselves and/or by the commercial cleaning reinforcing agents which contain between 4 and 30% and usually from 8 to 14% of their weight of water. Occasionally additional amounts of water are added (about 2 to 4% by weight relative to the textiles to be cleaned) to the cleaning bath containing the reinforcing agents in order to improve the cleaning effect relative to so-called "meager" soiling substances.
The invention also concerns a composition or bath useful in dry cleaning or de-oiling textiles, to prevent "greying" or redepositon of stains on textiles comprising natural, artificial or synthetic fibers or mixtures of such fibers, during the dry cleaning or de-oiling operations, by means of suitably stabilized perchloroethylene possibly containing up to 6% by weight water, with respect to the textiles to be treated and the usual auxiliary substances, more particularly cleaning reinforcing and anti-static agents, in which each of said auxiliary substances may be present in amounts from 1 to 10 g per liter of said composition, which composition is characterized in that it contains, besides the perchloroethylene and its suitable stabilization agents, 0,5 to 8% and preferably from 2 to 5% by weight relative to said composition of at least one monoketone having a boiling point below or equal to 160° C. and, preferably, less than 140° C.
The monoketone may be selected from among those represented by the general formula: ##STR2## where R and R' are as defined hereinabove.
The following are given by way of non-limiting examples illustrative of specific monoketones corresponding to the above general formula in which one or two or more thereof may be used in the practice of this invention: 2-propanone, 1-chloro,2-propanone, 1,1-dichloro-2-propanone, 1-bromo 2-propanone, 2-butanone,1-bromo 2-butanone, 1-butyne 3-one, 3-methyl 2-butanone, 3-methyl 3-butene 2-one, 3-pentene 2-one 2,4-dimethyl 3-pentanone, 4-methyl 3-pentene 2-one, 1-hexene 5-one, 2-hexanone, 3-hexanone, 5-methyl 2-hexanone, 5-methyl 3-hexanone, 4-heptanone, 2-methyl 4-heptanone, acetylcyclopropylketone, methylethylcyclopropylketone, methylethylcyclobutylketone, cyclopentanone, methylcyclopentanone and cyclohexanone.
In an advantageous embodiment of the invention, representative of the ketone used is 2-pentanone and/or 3-pentanone as the anti-redeposition additive.
In a preferred embodiment of the invention, the ketone used includes or consists essentially of 3--3 dimethyl 2-butanone.
The mode of operation permitting evaluation of the "greying" phenomenon of textiles, has been carried out through the use of a staining matter representative of a stain usually present on garments and having the following composition by weight:
______________________________________
Parts
______________________________________
Carpet beating dust screened at 26 mesh
(0.63 mm) 100
Oil drained from a car engine
100
Lampblack (50%) crushed in 30 SAE engine
oil (50%) 4
Oxyethylenated castor oil having 10 moles
ethylene oxide 5
Distilled water 50
Stabilized perchloroethylene
155
______________________________________
The samples of textiles studied were the following:
100% polyester weighing 268 g/m2
100% 6/6 polyamide weighing 170 g/m2
100% polyacrylonitrile weighing 220 g/m2
100% wool weighing 280 g/m2
100% cotton weighing 110 g/m2
In order to evaluate the "greying" of textiles, the following were successively introduced in a laboratory washing drum:
225 cm2 of each of the samples of textiles just mentioned
1 liter of stabilized perchloroethylene-based composition in which 0.5 g of the staining matter defined hereabove was dispersed therein.
After treatment at a bath temperature of about 25° C. for a period of 5 minutes, the textile samples were centrifuged and dried at a temperature of 60° C. in a ventilated oven.
Each of the samples treated in this way, and "greyed" to a greater or lesser extent, was subjected to an operation of determining the reflectance index by means of the "Reflection meter 670" of the company "Photovolt" (United States of America) provided with a green filter.
The apparatus was set to 100 for each untreated textile, and a reflectance index was measured for each "greyed" sample.
The less the "greying" phenomenon, the closer this index will be to the value of 100.
In the following examples, which illustrate the various aspects of the invention in non-limiting manner, the stated percentages of the components of each composition are expressed by weight of the considered composition.
Using the mode of operation set out above, the "anti-greying" effect or anti-redeposition effect was examined of a composition based on initially stabilized perchloroethylene to which 5% acetone was incorporated as the "anti-greying" additive.
The starting perchlorethylene was stabilized by 0.0025% of triethylamine, 0.002% of N-methylpyrrole and 0.02% of n-butanol.
Following Table 1 summarizes the results obtained. This table also shows a reference test carried out with a composition which did not contain acetone according to the invention.
TABLE 1
______________________________________
Measure of reflectance index
poly- polyacry-
poly-
cotton
wool ester lonitrile
amide
______________________________________
Reference 83 90 71.5 75 93
blank
Perchloroethy-
91.5 98.5 96 88 98.5
lene + 5% acetone
______________________________________
The same operational conditions as in Example 1 were applied but using 2-butanone instead of acetone. Following Table 2 sets forth the results obtained:
TABLE 2
______________________________________
Measure of reflectance index
poly- polyacry-
poly-
cotton
Wool ester lonitrile
amide
______________________________________
Reference 89 86.5 70 72 91
blank
Perchloroethy-
lene + 5% 2-bu-
90 97 90.5 80 97.5
tanone
______________________________________
Using the operational conditions as in Example 1, but in which the acetone was substituted by 3-methyl 2-butanone, the following results were obtained:
TABLE 3
______________________________________
Measure of reflectance index
polyacry-
poly-
cotton
wool polyester
lonitrile
amide
______________________________________
Reference 87 92 73 69 91
blank
Perchloroethy-
lene + 5%, 3-
87 98 82 77.5 97
methyl 2-butanone
______________________________________
By incorporating 3,3-dimethyl 2-butanone instead of acetone as anti-redeposition agent added to perchlorethylene stabilized as in Example 1, and by applying the same procedural steps as described in said example, the following results were observed:
TABLE 4
______________________________________
Measure of reflectance index
polyacry-
cotton
wool polyester
lonitrile
polyamide
______________________________________
Reference 89 86.5 70 72 91
blank
Perchloroethy- -lene + 5% 3,3-
90.5 96 83 79 97.5
dimethyl 2-buta-
none
______________________________________
Example 4 was repeated, but using a perchloroethylene base composition containing 2.5% of 3,3-dimethyl 2-butanone instead of 5%.
The results were the following:
TABLE 5
______________________________________
Measure of reflectance index
polyacry-
poly-
cotton
wool polyester
lonitrile
amide
______________________________________
Reference 83 90 71.5 75 93
blank
Perchloroethy-
lene + 2.5% 3,3-
87.5 98.5 78.0 86.5 98
dimethyl 2-buta-
none
______________________________________
Using a dry-cleaning composition consisting essentially of 95% perchloroethylene stabilized as in Example 2, and 5% 2-pentanone, and employing the same procedural steps as in Example 1, the following results were obtained:
TABLE 6
______________________________________
Measure of reflectance index
polyacry-
poly-
cotton
wool polyester
lonitrile
amide
______________________________________
Reference 89 86.5 70 72 91
blank
Perchloroethy-
lene + 5% 2-pen-
91.5 97.5 84 76 95
tanone
______________________________________
Example 6 was repeated with 3-pentanone instead of 2-pentanone as the anti-redeposition additive. Table 7 illustrates the results obtained.
TABLE 7
______________________________________
Measure of reflectance index
polyacry-
cotton
wool polyester
lonitrile
polyamide
______________________________________
Reference 89 86.5 70 72 91
blank
Perchloroethy-
lene + 5% 3-
92 97.5 85 81 99
pentanone
______________________________________
The same procedural steps as in Example 1 were applied except that the anti-redeposition additive was 4-methyl 2-penatnone. Table 8 illustrates the results secured:
TABLE 8
______________________________________
Measure of reflectance index
polyacry-
cotton
wool polyester
lonitrile
polyamide
______________________________________
Reference 89 86.5 70 72 91
blank
Perchloroethy-
lene + 5% 4-
90.5 98 87.5 80 97
methyl-2penta-
none
______________________________________
Example 8 was repeated but with only 2.5% instead of 5% 4-methyl 2-pentanone, in the dry cleaning composition.
TABLE 9
______________________________________
Measure of reflectance index
polyacry-
poly-
cotton
wool polyester
lonitrile
amide
______________________________________
Reference 87 92 73 69 92
blank
Perchloroethylene
+ 2.5% 4-methyl-
87 94 81 73 94.5
2-pentanone
______________________________________
The following results were obtained using the same operational conditions as in Example 1, but with a dry-cleaning composition consisting essentially of 95% perchloroethylene (stabilized as in Example 1) and 5% 2,4-dimethyl 3-pentanone (DMP):
TABLE 10
______________________________________
Measure of reflectance index
polyacry-
poly-
cotton
wool polyester
lonitrile
amide
______________________________________
Reference 80 90.5 73.5 73 91
blank
Perchloroethylene
86 89 74 85.5 98
+ 5% DMP
______________________________________
By replacing 2,4-dimethyl 3-pentanone of the preceding example by 4-heptanone, the results were as follows:
TABLE 11
______________________________________
Measure of reflectance index
polyacry-
poly-
cotton
wool polyester
lonitrile
amide
______________________________________
Reference 84 92 69 71 92
blank
Perchloroethylene
89 97 75 81 96
+5% 4-heptanone
______________________________________
By replacing 4-heptanone of the preceding example by cyclohexanone, the following results were observed:
TABLE 12
______________________________________
Measure of reflectance index
polyacry-
poly-
cotton
wool polyester
lonitrile
amide
______________________________________
Reference 89 86.5 70 72 92
blank
Perchloroethylene
89.5 97 86 83.5 93
+6% cyclohexa-
none
______________________________________
Above Examples 1-12 show in general the improvement in anti-redeposition which may be more marked, depending on the considered ketone and the treated textile material.
Claims (12)
1. A process for anti-redeposition, which has the effect of reducing greying by redeposition of staining substances on textiles of natural, synthetic or artificial fibers or mixtures thereof, in the course of operation of dry cleaning, or de-oiling by means of perchloroethylene, comprising incorporating in the perchloroethylene a sufficient anti-greying amount of at least one monoketone anti-redeposition additive having a boiling point which does not exceed 160° C. to observe the desired anti-redeposition effect.
2. A process as claimed in claim 1, in which the monoketone additive has a boiling point below 140° C.
3. An anti-redeposition process according to claim 1, in which the monoketone is a ketone represented by the general formula: ##STR3## wherein R and R' which may be identical or different represent C1 -C8 alkyl, C1 -C8 fluoro-, chloro- or bromo-alkyl, C2 -C8 alkenyl, C2 -C8 alkynyl or a cyclopropyl group, or taken jointly R and R' represent a C5 -C6 cycloalkyl group, a C5 -C8 alkylcycloalkyl or a C5 -C8 alkenylcycloalkyl group.
4. A process as claimed in claim 1, in which from 0.5 to 8% by weight of the anti-redeposition additive is incorporated in the perchloroethylene.
5. A process as claimed in claim 1, in which 2 to 5% by weight of the anti-redeposition additive is incorporated in the perchloroethylene.
6. A process as claimed in claim 1, in which the additive is 2-pentanone and/or 3-pentanone.
7. A process as claimed in claim 1, in which the additive is 3,3-dimethyl 2-butanone.
8. An anti-redeposition composition for dry cleaning or de-oiling based on stabilized perchloroethylene, which may contain water up to 6% by weight relative to the textiles to be treated, and auxiliary substances, including cleaning reinforcing agents and anti-static agents, each of which substances may be present in an amount of from 1 to 10 g per liter of said composition, characterized in that the composition contains from 0.5 to 8% by weight of at least one monoketone anti-redeposition additive having a boiling point below or equal to 160° C.
9. A composition as claimed in claim 8, in which the monoketone has a boiling point below 140° C.
10. An anti-redeposition composition as claimed in claim 8, in which the monoketone anti-redeposition additive is represented by the general formula: ##STR4## wherein R and R' which may be identical or different represent C1 -C8 alkyl, C1 -C8 fluoro-, chloro- or bromo-alkyl, C2 -C8 alkenyl, C2 -C8 alkynyl or a cyclopropyl group, or taken jointly R and R' represent a C5 -C6 cycloalkyl group, a C5 -C8 alkylcycloalkyl or a C5 -C8 alkenylcycloalkyl group.
11. An anti-redeposition composition as claimed in claim 8, in which the monoketone additive is 2-pentanone and/or 3-pentanone.
12. An anti-redeposition composition as claimed in claim 8, in which the monoketone additive is 3,3-dimethyl 2-butanone.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR7819589 | 1978-06-30 | ||
| FR7819589A FR2429862A1 (en) | 1978-06-30 | 1978-06-30 | PROCESS AND COMPOSITIONS FOR CLEANING AND DESENSING OF TEXTILE MATERIALS |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US4227883A true US4227883A (en) | 1980-10-14 |
Family
ID=9210177
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US05/956,627 Expired - Lifetime US4227883A (en) | 1978-06-30 | 1978-11-01 | Process and composition for cleaning or de-oiling textile materials |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US4227883A (en) |
| JP (1) | JPS595240B2 (en) |
| BE (1) | BE871619A (en) |
| BR (1) | BR7807239A (en) |
| CA (1) | CA1102968A (en) |
| CH (1) | CH635880A5 (en) |
| DE (1) | DE2846982C2 (en) |
| FR (1) | FR2429862A1 (en) |
| GB (1) | GB2024241B (en) |
| IT (1) | IT1109224B (en) |
| NL (1) | NL7810927A (en) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4378968A (en) * | 1980-06-20 | 1983-04-05 | Chloe Chimie | Process for preventing the redeposition of soil during dry cleaning, and composition for carrying out this process |
| US5534743A (en) * | 1993-03-11 | 1996-07-09 | Fed Corporation | Field emission display devices, and field emission electron beam source and isolation structure components therefor |
| US5548181A (en) * | 1993-03-11 | 1996-08-20 | Fed Corporation | Field emission device comprising dielectric overlayer |
| US5561339A (en) * | 1993-03-11 | 1996-10-01 | Fed Corporation | Field emission array magnetic sensor devices |
| US5629583A (en) * | 1994-07-25 | 1997-05-13 | Fed Corporation | Flat panel display assembly comprising photoformed spacer structure, and method of making the same |
| US5903098A (en) * | 1993-03-11 | 1999-05-11 | Fed Corporation | Field emission display device having multiplicity of through conductive vias and a backside connector |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2021090910A1 (en) * | 2019-11-08 | 2021-05-14 | セントラル硝子株式会社 | Molecular structure altering agent for detecting protein aggregates, detection method thereof, medical equipment cleaning agent, soil cleaning agent and soil cleaning method |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1386783A (en) | 1963-03-13 | 1965-01-22 | Hoechst Ag | Chemical cleaning of fibrous materials |
| FR1536343A (en) | 1965-02-08 | 1968-08-10 | Dow Chemical Co | Textile cleaning process |
| US3481685A (en) * | 1965-03-11 | 1969-12-02 | Ici Ltd | Process for the treatment of textile materials |
| US4014805A (en) * | 1975-11-28 | 1977-03-29 | Fmc Corporation | Dry cleaning formulation |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3564063A (en) * | 1958-02-03 | 1971-02-16 | Ppg Industries Inc | Stabilized methylchloroform compositions |
| GB1296837A (en) * | 1969-04-29 | 1972-11-22 | ||
| BE755668A (en) * | 1970-09-03 | 1971-03-03 | Solvay | PROCESS FOR STABILIZING 1,1,1-TRICHLORETHANE. |
| BE756709A (en) * | 1970-09-28 | 1971-03-25 | Solvay | PROCESS FOR STABILIZING 1,1,1-TRICHLORETHANE. |
-
1978
- 1978-06-30 FR FR7819589A patent/FR2429862A1/en active Granted
- 1978-10-27 BE BE191418A patent/BE871619A/en not_active IP Right Cessation
- 1978-10-28 DE DE2846982A patent/DE2846982C2/en not_active Expired
- 1978-10-31 IT IT51718/78A patent/IT1109224B/en active
- 1978-11-01 US US05/956,627 patent/US4227883A/en not_active Expired - Lifetime
- 1978-11-01 BR BR7807239A patent/BR7807239A/en unknown
- 1978-11-02 CA CA315,759A patent/CA1102968A/en not_active Expired
- 1978-11-02 GB GB7843041A patent/GB2024241B/en not_active Expired
- 1978-11-02 NL NL7810927A patent/NL7810927A/en not_active Application Discontinuation
- 1978-11-02 CH CH1131178A patent/CH635880A5/en not_active IP Right Cessation
-
1979
- 1979-03-01 JP JP54022612A patent/JPS595240B2/en not_active Expired
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1386783A (en) | 1963-03-13 | 1965-01-22 | Hoechst Ag | Chemical cleaning of fibrous materials |
| FR89341E (en) | 1963-03-13 | 1967-06-09 | Hoechst Ag | Chemical cleaning of fibrous materials |
| FR1536343A (en) | 1965-02-08 | 1968-08-10 | Dow Chemical Co | Textile cleaning process |
| US3481685A (en) * | 1965-03-11 | 1969-12-02 | Ici Ltd | Process for the treatment of textile materials |
| US4014805A (en) * | 1975-11-28 | 1977-03-29 | Fmc Corporation | Dry cleaning formulation |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4378968A (en) * | 1980-06-20 | 1983-04-05 | Chloe Chimie | Process for preventing the redeposition of soil during dry cleaning, and composition for carrying out this process |
| US5534743A (en) * | 1993-03-11 | 1996-07-09 | Fed Corporation | Field emission display devices, and field emission electron beam source and isolation structure components therefor |
| US5548181A (en) * | 1993-03-11 | 1996-08-20 | Fed Corporation | Field emission device comprising dielectric overlayer |
| US5561339A (en) * | 1993-03-11 | 1996-10-01 | Fed Corporation | Field emission array magnetic sensor devices |
| US5587623A (en) * | 1993-03-11 | 1996-12-24 | Fed Corporation | Field emitter structure and method of making the same |
| US5903098A (en) * | 1993-03-11 | 1999-05-11 | Fed Corporation | Field emission display device having multiplicity of through conductive vias and a backside connector |
| US5903243A (en) * | 1993-03-11 | 1999-05-11 | Fed Corporation | Compact, body-mountable field emission display device, and display panel having utility for use therewith |
| US5629583A (en) * | 1994-07-25 | 1997-05-13 | Fed Corporation | Flat panel display assembly comprising photoformed spacer structure, and method of making the same |
Also Published As
| Publication number | Publication date |
|---|---|
| GB2024241B (en) | 1982-10-06 |
| FR2429862A1 (en) | 1980-01-25 |
| GB2024241A (en) | 1980-01-09 |
| JPS556567A (en) | 1980-01-18 |
| JPS595240B2 (en) | 1984-02-03 |
| BR7807239A (en) | 1980-05-06 |
| CA1102968A (en) | 1981-06-16 |
| IT7851718A0 (en) | 1978-10-31 |
| CH635880A5 (en) | 1983-04-29 |
| DE2846982C2 (en) | 1982-09-30 |
| DE2846982A1 (en) | 1980-01-17 |
| NL7810927A (en) | 1980-01-03 |
| FR2429862B1 (en) | 1980-11-28 |
| BE871619A (en) | 1979-04-27 |
| IT1109224B (en) | 1985-12-16 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US5888250A (en) | Biodegradable dry cleaning solvent | |
| US3872021A (en) | Cleaning composition | |
| US3042479A (en) | Chlorofluorohydrocarbons in dry cleaning compositions and process | |
| US4227883A (en) | Process and composition for cleaning or de-oiling textile materials | |
| DE2004232C3 (en) | Process for dry cleaning of textiles | |
| US4077770A (en) | Textile cleaning process including soil-repellent finish | |
| US3708260A (en) | Textile treatment process | |
| US4378968A (en) | Process for preventing the redeposition of soil during dry cleaning, and composition for carrying out this process | |
| US3954647A (en) | Industrial drycleaning detergent | |
| US4220448A (en) | Process for dry-cleaning or de-oiling by means of a perchloroethylene base composition | |
| US3772205A (en) | Cleaning agent for textiles | |
| US20090031504A1 (en) | Method for Chemically Cleaning Textile Material | |
| DE2656384B2 (en) | Process for cleaning textiles in organic solvent baths | |
| US3628911A (en) | Textile chemical cleaning processes | |
| US3030172A (en) | Dry cleaning process and composition | |
| US2904514A (en) | Textile cleaning solution | |
| JPH10110195A (en) | Composition suitable for use in pretreatment of fiber | |
| US3692686A (en) | Novel non-flammable azeotrope solvent composition | |
| GB2031940A (en) | Cleaning and deoiling of textile materials using perchloroethylene | |
| DE2028727A1 (en) | ||
| US3505005A (en) | Dry cleaning method | |
| SE176728C1 (en) | ||
| DD254746A1 (en) | DETERGENT FOR POLYESTER TEXTILES | |
| WO1994001522A1 (en) | 1,1-dichloro-1-fluoroethane based dry cleaning composition | |
| GB2161497A (en) | Method of producing oil-containing cleaning fibres |